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0-2 years
Not Disclosed
10 Sept. 17, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title:

CTM II – Clinical Trial Manager

Location:

Remote – Pennsylvania, USA

Job ID:

25101804

Company Overview:

Syneos Health® is a fully integrated biopharmaceutical solutions organization that accelerates customer success by combining clinical, medical affairs, and commercial expertise. Our Clinical Development model centers on patients and customers, streamlining processes to deliver therapies efficiently.

Learn more: Syneos Health


Job Summary:

The CTM II is responsible for the development, coordination, and implementation of Phase 1 clinical research studies at the organization’s facilities. This role oversees logistics, study progress, compliance, and team management to ensure high-quality, timely, and compliant research outcomes.


Key Responsibilities:

  • Develop, coordinate, and implement Phase 1 clinical research studies according to protocols and timelines.

  • Collaborate with the principal investigator to design study protocols and ensure scientific integrity.

  • Serve as liaison between research subjects, client teams, investigators, and clinic operations teams to facilitate communication and coordination.

  • Plan logistics and resource usage, including scheduling, staffing, and equipment needs.

  • Track study progress in alignment with project milestones, client deliverables, and budget; provide regular updates to stakeholders.

  • Ensure compliance with global and regional regulations, including Good Clinical Practice (GCP) guidelines.

  • Supervise experienced support staff and/or entry-level team members, prioritizing and directing tasks for efficient workflow.

  • Deliver operational results that moderately impact team and organizational success.

  • Adapt new procedures, techniques, and tools to improve clinical trial processes and outcomes.

  • Apply basic management practices, including work scheduling, task prioritization, coaching, and process execution.


Qualifications:

  • Broad operational, administrative, and/or specialized knowledge in clinical trial management.

  • Practical experience in executing processes, projects, and tactical initiatives within a team.

  • Awareness of the impact of work on related areas and overall study outcomes.


Certifications:

  • Relevant certifications in clinical trial management or related fields preferred.


Skills & Competencies:

  • Strong leadership and management abilities.

  • Excellent communication and collaboration skills.

  • Effective planning and prioritization.

  • Proficiency in tracking, reporting, and analyzing study progress.

  • Knowledge of global and regional regulations governing clinical trials.


Impact and Contribution:

  • Roles at the M23 level significantly contribute to the success of clinical research studies by managing resources, coordinating teams, and ensuring protocol adherence.

  • Provides strategic and tactical direction to achieve operational results and facilitate timely, high-quality research.

  • Supports the advancement of medical knowledge and development of new treatments.


Job Category:

  • Clinical Trial Management / Clinical Operations / Phase 1 Clinical Research